The association between glucose‐dependent insulinotropic polypeptide and/or glucagon‐like peptide‐1 receptor agonist prescriptions and substance‐related outcomes in patients with opioid and alcohol use disorders: A real‐world data analysis

Aims: This study aimed to estimate the strength of association between prescriptions of glucose‐dependent insulinotropic polypeptide (GIP) and/or glucagon‐like peptide‐1 receptor agonists (GLP‐1 RA) and the incidence of opioid overdose and alcohol intoxication in patients with opioid use disorder (O...

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Publicado en:Addiction Vol. 120; no. 2; pp. 236 - 251
Autores principales: Qeadan, Fares, McCunn, Ashlie, Tingey, Benjamin
Formato: research tables/charts Journal Article
Publicado: Wiley-Blackwell Feb2025
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Feb2025
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      pub: Wiley-Blackwell
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        atl: The association between glucose‐dependent insulinotropic polypeptide and/or glucagon‐like peptide‐1 receptor agonist prescriptions and substance‐related outcomes in patients with opioid and alcohol use disorders: A real‐world data analysis
      aug:
        au:
          Qeadan, Fares
          McCunn, Ashlie
          Tingey, Benjamin
        affil: Parkinson School of Health Sciences and Public Health, Loyola University Chicago, Maywood IL, , USA
      sug:
        subj:
          Substance Use Disorders Drug Therapy
          Alcohol Abuse Drug Therapy
          Glucagon-Like Peptide-1 Receptor Agonists Therapeutic Use
          Peptides Therapeutic Use
          Drugs, Prescription
          Treatment Outcomes
          Human
          Male
          Female
          Middle Age
          Aged
          Retrospective Design
          Record Review
          Prospective Studies
          Descriptive Statistics
          Confidence Intervals
          Comorbidity
          Opiate Overdose
          Alcoholic Intoxication
          Obesity
          Diabetes Mellitus, Type 2
          Middle Aged: 45-64 years
          Aged: 65+ years
          Male
          Female
      ab: Aims: This study aimed to estimate the strength of association between prescriptions of glucose‐dependent insulinotropic polypeptide (GIP) and/or glucagon‐like peptide‐1 receptor agonists (GLP‐1 RA) and the incidence of opioid overdose and alcohol intoxication in patients with opioid use disorder (OUD) and alcohol use disorder (AUD), respectively. This study also aimed to compare the strength of the GIP/GLP‐1 RA and substance use‐outcome association among patients with comorbid type 2 diabetes and obesity. Design: A retrospective cohort study analyzing de‐identified electronic health record data from the Oracle Cerner Real‐World Data. Setting: About 136 United States of America health systems, covering over 100 million patients, spanning January 2014 to September 2022. Participants: The study included 503 747 patients with a history of OUD and 817 309 patients with a history of AUD, aged 18 years or older. Measurements The exposure indicated the presence (one or more) or absence of GIP/GLP‐1 RA prescriptions. The outcomes were the incidence rates of opioid overdose in the OUD cohort and alcohol intoxication in the AUD cohort. Potential confounders included comorbidities and demographic factors. Findings Patients with GIP/GLP‐1 RA prescriptions demonstrated statistically significantly lower rates of opioid overdose [adjusted incidence rate ratio (aIRR) in OUD patients: 0.60; 95% confidence interval (CI) = 0.43–0.83] and alcohol intoxication (aIRR in AUD patients: 0.50; 95% CI = 0.40–0.63) compared to those without such prescriptions. When stratified by comorbid conditions, the rate of incident opioid overdose and alcohol intoxication remained similarly protective for those prescribed GIP/GLP‐1 RA among patients with OUD and AUD. Conclusions: Prescriptions of glucose‐dependent insulinotropic polypeptide and/or glucagon‐like peptide‐1 receptor agonists appear to be associated with lower rates of opioid overdose and alcohol intoxication in patients with opioid use disorder and alcohol use disorder. The protective effects are consistent across various subgroups, including patients with comorbid type 2 diabetes and obesity.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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